FDA Inspection
Ormco/SybronendoOrmco/Sybronendo – FDA Inspection, Jul 21, 2017
Record Details
This FDA Inspection record concerns Ormco/Sybronendo, with an inspection on July 21, 2017, issued by the Los Angeles District Office, covering medical devices & rad health.
- Company
- Ormco/Sybronendo
- Inspection Date
- July 21, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · ba06a9d2-0e49-4892-abf3-533c1286dc95
Inspection Facts
- Inspection number
- 1031062
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Ormco/Sybronendo
3| Date | Classification | Office | Project area |
|---|---|---|---|
| January 24, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 29, 2011 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 20, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Ormco/Sybronendo
- FDA Inspection 763710 - 2012-01-24
- FDA Inspection 731636 - 2011-06-29
- FDA Inspection 641489 - 2010-01-20
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